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The difference in shoal size of P. reticulata between the two flow conditions may be explained by energetic allocation.
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The differences observed between the brain and liver may be explained by different energetic requirements and organ cell composition.
We argue this could be unintentionally causing the pattern of outbreeding, although the heterozygosity correlation may instead be explained by the energetic costs associated with larger body size.
The interdependency between the changes in the substrate sequence in response to the drug-induced protease mutations can be explained by the energetic fitness of the sequences to the structural space of HIV-1 protease.
These differences could be explained by the additional energetic consumption for cell growth in pure cultures that is negligible in both mixed cultures.
This behaviour can be explained by different sources for the input of energetic particles into the growing film for RF and DC excitation.
The measured energetic oxygen ions in the cusp cannot be explained by a ring current source.
This can be explained by the addition of a 3He-enrich component related to solar energetic particle events such as flare events.
The higher MO2Rest of Heron Island populations could also be explained by such differences, because a larger gill surface area will lead to higher energetic costs for maintaining ion-homeostasis [40] and a higher red blood cell content leads to increased blood viscosity and therefore higher energetic costs for maintaining blood circulation.
The above-mentioned difference in ATP production per acetate can be explained by the postulated additional coupling of methylene-THF reduction to the reduction of ferredoxin (or an energetic equivalent) in a second electron bifurcating reaction in M. thermoacetica.
This can be explained by multiple possibilities.
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